M. domestica is the most important insect that transmit pathogens for diseases in the world. The use of nanotechnology is eco-friendly method in control pests. The study aims to investigate the feasibility of bio-manufacturing nanocapsules of fungal secondary metabolites in order to improve the efficiency of metabolite and assess their inhibitory effect on the acetylcholine esterase enzyme in housefly larvae. An equal mixture of organic solvents, ethyl acetate and dichloromethane, was used to extract the metabolic products of the fungus M. anisopliae, (PEG4000) and chitosan was used in the preparation of nanocapsules. The results of the DLS granular size assay showed that the size of the extract particles and the size of the chitosan and (PEG 4000) nanocapsules were 610, 217 and 188 nm, respectively. The SEM images showed that the diameter of the extract and the nanocapsules chitosan and polyethylene glycol 4000 reached a rate 547.5, 17.8 and 26.2 nm, respectively. The FTIR showed that the extract of the second products of the fungus contains functional groups like: alkynes and alkenes, amines, carboxyl and aromatic groups, while the presence of groups of phenols, alcohol, amines, alkenes, and alkyl halides was recorded for nanocapsules of chitosan and PEG. The results showed that the extract of fungal metabolic and nanocapsules has an inhibitory effect on acetylcholinesterase enzyme and reached the highest inhibition rate 53.2 ,36.3,18.2% when treated with nanocapsules PEG at a concentration 500 ppm, extract of fungal metabolites at a concentration 50,000 ppm, chitosan nanocapsules at a concentration 500 ppm respectively. It is clear that acetylcholinesterase inhibition is one of the mechanisms of fungi metabolic action and the nanocapsules prepared from them.

The house flies Musca domestica )Diptera:musidae) are the primary carrier of many pathogens such as cholera, typhoid, anthrax, and others. The use of chemical pesticides as a basic method of control leads to many problems at the environmental and health level. The use of safe alternatives to chemical pesticides has become an urgent necessity. The research aims to find biological alternatives that are environment-friendly and non-pathogenic to humans in controlling house flies through the possibility of extracting and diagnosing some secondary metabolites produced by the fungus Metarhizium anisopliae and testing their effects on the second larval stage of house flies using different treatment methods that include direct spraying of the larvae, treating the food environment, and the dipping method. Secondary metabolites and toxins of Metarhizium anisopliae were extracted in liquid media PDB using a mixture of organic solvents such as ethyl acetate and methanol. The secondary metabolites were identified by gas chromatography-mass spectrometry (GC-MS). The results showed the identification of 10 chemical compounds, including phenol, 2,4-bis(1,1-dimethylethyl (C14H22O)., Diethyl Phthalate (C12H14O4),  Hexadecanoic acid, methyl ester (C17H34O2 ),  Phthalic acid, butyl undecyl ester (C23H36O4) , 9,12-Octadecanoic (Z,Z )-, methyl ester ( C19H34O2),  9-Octadecanoic acid, methyl ester, (C19H36O2), 9,12,15-Octadecanoic acid,methyl ester,(Z,Z,Z) (C19H32O2), Octadecanoic acid,methyl ester(C19H38O2), Oleic Acid (C24H38O4), 9-Octadecanoic acid (Z)-,2-hydroxyl (hydroxymethyl) ethyl ester(C21H40O4) ,and Di-n-octyl phthalate (C24H38O4 ). The results showed that the crude extract of the fungus cause the best mortality rate  in the second instar larvae at concentrations of 3 and 5% after 72 hours of treatment when  the mortality rates ranged between 60-100%. The mortality rates were directly proportional to the increase in concentration and time with a significant difference. The results also showed that the treatment of the food media was the most effective in affecting the larvae of flies, recording mortality rates that reached 100%, with a significant difference with direct spraying and dipping methods. These results reveal the significant efficacy of the tested secondary metabolite crude of m.anesopalae against Musca domestica which could be used as an ecofriendly alternative for insect control.

The current study aims to show the importance of plant products as mosquitocides against Culex quinquefasciatus. Castor oil Nanoemulsions were subedit in various ratios including castor oil, ethanol, tween 80, and deionized water by using ultrasonication. Thermodynamic, centrifugation, PH, assay which improved that the formula  of 10 ml  of castor  oil, ethanol  5ml, tween 80 (14 ml) and deionized water 71ml was more stable than other formulas. The stable formula of castor oil nanoemulsion was characterized by transmission electron microscopy (TEM) and dynamic light scattering (DLS). Nanoemulsion droplets were spherical in shape and were found to have a Z-average diameter of 87.4nm. A concentration of castor oil nanoemulsion 250, 350, 450, and 550 ppm were tested as larvicidal agents and bulk emulsion 1000, 1500, 2000 , and 2500 ppm were tested also and compared, against the fourth instar larvae of C. quinquefasciatus. Castor oil nanoemulsion exhibited higher activity when compared to bulk emulsion. LC50 of castor oil nanoemulsion and castor bulk emulsion were found as 291.46 and 439.19ppm after 72 h, respectively. The toxic effects of castor oil bulk and Nano emulsion was tested against non-target organism Guppy fish and found to be not toxic at the concentration which used in the study.